Author
Listed:
- Xuehan Zhou
(University of Zürich
University and ETH Zürich)
- Carrie Stine
(University of Washington
University of Washington
University of Washington School of Medicine)
- Patricia Oliveira Prada
(Max Planck Institute for Metabolism Research
University of Cologne
State University of Campinas (UNICAMP))
- Debora Fusca
(University of Cologne
University of Cologne)
- Kevin Assoumou
(University of Geneva)
- Jan Dernic
(University of Zürich)
- Musadiq A. Bhat
(University of Zürich)
- Ananya S. Achanta
(University of Washington
University of Washington)
- Joseph C. Johnson
(University of Washington
University of Washington)
- Amanda Loren Pasqualini
(University of Washington
University of Washington)
- Sanjana Jadhav
(University of Washington
University of Washington)
- Corinna A. Bauder
(Max Planck Institute for Metabolism Research
University of Cologne)
- Lukas Steuernagel
(Max Planck Institute for Metabolism Research
University of Cologne)
- Luca Ravotto
(University of Zürich)
- Dietmar Benke
(University of Zürich
University and ETH Zürich)
- Bruno Weber
(University of Zürich
University and ETH Zürich)
- Azra Suko
(University of Washington
University of Washington)
- Richard D. Palmiter
(University of Washington
University of Washington)
- Miriam Stoeber
(University of Geneva)
- Peter Kloppenburg
(University of Cologne
University of Cologne)
- Jens C. Brüning
(Max Planck Institute for Metabolism Research
University of Cologne
University Hospital Cologne)
- Michael R. Bruchas
(University of Washington
University of Washington
University of Washington School of Medicine)
- Tommaso Patriarchi
(University of Zürich
University and ETH Zürich)
Abstract
Nociceptin/orphanin-FQ (N/OFQ) is a recently appreciated critical opioid peptide with key regulatory functions in several central behavioral processes including motivation, stress, feeding, and sleep. The functional relevance of N/OFQ action in the mammalian brain remains unclear due to a lack of high-resolution approaches to detect this neuropeptide with appropriate spatial and temporal resolution. Here we develop and characterize NOPLight, a genetically encoded sensor that sensitively reports changes in endogenous N/OFQ release. We characterized the affinity, pharmacological profile, spectral properties, kinetics, ligand selectivity, and potential interaction with intracellular signal transducers of NOPLight in vitro. Its functionality was established in acute brain slices by exogeneous N/OFQ application and chemogenetic induction of endogenous N/OFQ release from PNOC neurons. In vivo studies with fibre photometry enabled direct recording of NOPLight binding to exogenous N/OFQ receptor ligands, as well as detection of endogenous N/OFQ release within the paranigral ventral tegmental area (pnVTA) during natural behaviors and chemogenetic activation of PNOC neurons. In summary, we show here that NOPLight can be used to detect N/OFQ opioid peptide signal dynamics in tissue and freely behaving animals.
Suggested Citation
Xuehan Zhou & Carrie Stine & Patricia Oliveira Prada & Debora Fusca & Kevin Assoumou & Jan Dernic & Musadiq A. Bhat & Ananya S. Achanta & Joseph C. Johnson & Amanda Loren Pasqualini & Sanjana Jadhav &, 2024.
"Development of a genetically encoded sensor for probing endogenous nociceptin opioid peptide release,"
Nature Communications, Nature, vol. 15(1), pages 1-20, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-49712-0
DOI: 10.1038/s41467-024-49712-0
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